Canonical Allele Identifier: CA1528880922

Gene: ANKH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14717013G= , CM000667.2:g.14717013G=	GRCh38
NC_000005.9:g.14717122G= , CM000667.1:g.14717122G=	GRCh37
NC_000005.8:g.14770122G=	NCBI36
NG_008273.1:g.159766C=
NG_008273.2:g.159773C=
NG_051625.1:g.61220G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.1012-178C= MANE Select	ENSP00000284268.6:n.1012-178C=
ENST00000284268.6:c.1012-178C=	ENSP00000284268.6:n.1012-178C=
ENST00000502585.1:n.76C=
NM_054027.4:c.1012-178C=	NP_473368.1:n.1012-178C=
NM_054027.5:c.1012-178C=	NP_473368.1:n.1012-178C=
XM_017009644.2:c.928-178C=	XP_016865133.1:n.928-178C=
NM_054027.6:c.1012-178C= MANE Select	NP_473368.1:n.1012-178C=